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CPSF30 and Wdr33 directly bind to AAUAAA in mammalian mRNA 3′ processing

机译:CPSF30和WDR33直接与哺乳动物mRNA 3'加工中的aauaaa结合

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摘要

AAUAAA is the most highly conserved motif in eukaryotic mRNA polyadenylation sites and, in mammals, is specifically recognized by the multisubunit CPSF (cleavage and polyadenylation specificity factor) complex. Despite its critical functions in mRNA 3′ end formation, the molecular basis for CPSF–AAUAAA interaction remains poorly defined. The CPSF subunit CPSF160 has been implicated in AAUAAA recognition, but direct evidence has been lacking. Using in vitro and in vivo assays, we unexpectedly found that CPSF subunits CPSF30 and Wdr33 directly contact AAUAAA. Importantly, the CPSF30–RNA interaction is essential for mRNA 3′ processing and is primarily mediated by its zinc fingers 2 and 3, which are specifically targeted by the influenza protein NS1A to suppress host mRNA 3′ processing. Our data suggest that AAUAAA recognition in mammalian mRNA 3′ processing is more complex than previously thought and involves multiple protein–RNA interactions.
机译:Aauaaa是真核mRNA多腺苷酸化位点中最高度保守的主题,并且在哺乳动物中,通过多管CPSF(裂解和多腺苷酸特异性因子)复合物特异性地认识。 尽管其在mRNA 3'结束地层中的关键功能,但CPSF-AauaAA相互作用的分子基础仍然仍然不足。 CPSF亚基CPSF160涉及Aauaaa认可,但缺乏直接证据。 在体外和体内测定中使用,我们意外地发现CPSF亚基CPSF30和WDR33直接联系AauaAA。 重要的是,CPSF30-RNA相互作用对于mRNA 3'加工至关重要,主要由其锌指2和3介导,其特异性地由流感蛋白NS1a抑制宿主mRNA 3'加工。 我们的数据表明,哺乳动物mRNA 3'加工中的AauaAA识别比以前认为更复杂,并且涉及多种蛋白质-RNA相互作用。

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